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PGT-M conditions

This table shows all PGT-M conditions currently approved and awaiting consideration by the HFEA.

Please note that we are updating this database, and some approved conditions may not be displayed. If you are unsure if a condition has been approved or not, please contact pgtm@hfea.gov.uk.

Download full approved condition list.

Condition name Status OMIM number Documents
Glycogen Storage Disease Type 4, (GSD4) approved 232500
Glycogen Storage Disease Type Ia approved 232200
Glycogen storage disease V (GSD5) approved 232600
Glycogen storage disease VI (GSD6) approved 232700
Glycogen storage disease VII (GSD7) approved 232800
Goiter, Multinodular 1, with or without Sertoli-Leydig cell tumours (MNG1) approved 138800
Gonadal mosaicism approved
Gorlin Syndrome approved 109400
Greig Cephalopolysyndactyly (GCPS) approved 175700
GRN-related Frontotemporal Lobar Degeneration with TDP43 inclusions approved 607485
Haemoglobin SC disease approved 141900.0038
Haemophilia A (HEMA) approved 306700
Haemophilia B (HEMB) approved 306900
Hajdu-Cheney Syndrome (HJCYS) approved 102500
HAJDU-CHENEY SYNDROME; HJCYS awaiting approval 102500
Harel-Yoon Syndrome, (HAYOS) approved 617183
Heimler Syndrome 1 approved 234580
Heimler Syndrome 2 approved 616617
Hereditary Angioedema (HAE) Type I & Type II approved 106100
Hereditary Angioedema (HAE) Type III approved 610618